FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
AB BELT PRO
K Number: K020429
·
Decision Sep 13, 2002
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
161
Applicant Total
3
Review Days
217
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Basic Information
- Device Name
- AB BELT PRO
- K Number
- K020429
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 890.5850
- Medical Specialty
- Physical Medicine
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- The Dezac Group
- Date Received
- February 8, 2002
- Decision Date
- September 13, 2002
- Product Code
- NGX
- Advisory Committee
- Physical Medicine
- Review Advisory Committee
- PM
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| NGX | Stimulator, Muscle, Powered, For Muscle Conditioning | FDA class 2 | Physical Medicine |
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